Assist with the day-to-day operations of clinical trials and
studies.
Participate in subject recruitment efforts, including educating
potential subjects on the details of the studies through phone
contacts, electronic contact, and/or personal interviews,
communicating with patients, and all pre-screening/screening
activities.
Obtain study subject's medical history and current medication
information, review research protocol inclusion/exclusion criteria,
and confirm eligibility of subject to participate in a study
clinical trial.
Perform informed consent process or ensure that the informed
consent process has occurred, is properly documented, and that
informed consent form documents are filed as required.
Interview prospective subjects for a variety of research
clinical trials. Educate potential subjects on the details of the
studies through phone contacts and personal interviews.
Schedule subject participation in research clinical trials,
coordinating availability of necessary space and clinical research
support (e.g., physician, nurse practitioner, laboratory,
radiology, pharmacy).
Collect, code, and analyze data obtained from research in an
accurate and timely manner.
Adhere to research regulatory standards.
Maintain detailed records of studies to ensure compliance with
requirements of the Food and Drug Administration (FDA), study
protocols, department, hospital/clinical standard operating
procedures, and/or other regulatory guidelines.
Participate in subject recruitment efforts, including
communicating with patients expressing an interest and all
pre-screening/screening activities.
Ensure that the necessary supplies and equipment for studies
are in stock and in working order.
Maintain familiarity with study protocols and documents of
assigned research studies.
Inventory, handle, and maintain accountability for study
supplies and investigational products in collaboration with
research pharmacy.
Perform data and sample collection at in-person and telephone
research visits.
Blood and tissue specimen handling and processing.
Enter data and send to coordinating center.
Work as a team member in coordination of assigned primary
studies.
Participant recruitment, consent, and retention.
Work with investigators and other staff to prepare IRB
submission and maintain study approval and certification.
Maintain individual certifications needed to perform study
duties (e.g., CITI trainings, coordinating center trainings,
central and local IRB trainings).
Work Location:
Onsite – this role is expected to work onsite and is located
in
Aurora, CO .
Why Join Us:
The University of Colorado Anschutz Medical Campus is a public
education, clinical, and research facility serving 4,500 students
and is a world-class medical destination at the forefront of
life-changing science, medicine, and healthcare. CU Anschutz offers
more than 42 highly rated degree programs through 6 schools and
colleges and receives over $500 million in research awards each
year. We are the single largest health professions education
provider in Colorado, awarding nearly 1,450 degrees annually.
Powered by our award-winning faculty, renowned researchers, and a
reputation for academic excellence, the CU Anschutz Medical Campus
drives innovation from the classroom to the laboratory to the
delivery of unparalleled patient care.
Why work for the University?
We have AMAZING benefits and offer exceptional amounts of holiday,
vacation, and sick leave! The University of Colorado offers an
excellent benefits package, including:
- Medical: Multiple plan options
- Dental: Multiple plan options
- Additional Insurance: Disability, Life, Vision
- Retirement 401(a) Plan: Employer contributes 10% of your gross
pay
- Paid Time Off: Accruals over the year
- Vacation Days: 22/year (maximum accrual 352 hours)
- Sick Days: 15/year (unlimited maximum accrual)
- Holiday Days: 15/year
- Tuition Benefit: Employees have access to this benefit on all
CU campuses
- ECO Pass: Reduced-rate RTD Bus and light rail service
There are many additional perks & programs with the
CU Advantage .
Qualifications:
Minimum Qualifications:
- Bachelor's degree in any field.
- Substitution: A combination of education and related
technical/military/paraprofessional experience may be substituted
for a bachelor's degree on a year-for-year basis.
Applicants must meet minimum qualifications at the time of
hire.
Preferred Qualifications:
- Bachelor's degree in science or health-related field.
- Clinical research or related experience.
- Experience with electronic data capture systems (e.g., EMR or
EHR and data management systems).
- Fluent in Spanish.
- Experience using REDCap, Epic, and/or OnCore.
- Experience with diabetes, obesity and/or human
physiology.
Conditions of Employment:
- Applicants must be legally authorized to work in the United
States without requiring sponsorship. We are unable to provide work
visa sponsorship or employment authorization for this position now
or in the future.
- Must be willing and able to pass national criminal and sex
offender background checks.
- Must successfully pass a 10-panel drug screen through
Children's Hospital Colorado.
*For questions regarding Children's Hospital drug testing
requirements, please contact Children's Human Resources at
720-777-8598. Some positions may require testing if access to
Children's Hospital or its systems is needed at any time during
employment with the University. If drug testing is required, it
will be listed in the job posting.
Knowledge, Skills, and Abilities:
- Knowledge and understanding of federal regulations and Good
Clinical Practice (GCP).
- Ability to communicate effectively, both in writing and
orally.
- Ability to establish and maintain effective working
relationships with employees at all levels throughout the
institution.
- Outstanding recruiting and customer service skills.
- Ability to multi-task to keep track of multiple participants'
schedules longitudinally.
- Knowledge of basic human anatomy, physiology, and medical
terminology.
- Ability to interpret and master complex research protocol
information.
- Ability to handle both blood and laboratory specimens for
processing.
- Knowledge of obesity and diabetes physiology.
- Ability to enter data effectively and efficiently.
- Strong interpersonal and communication skills, both in writing
and orally.
- Effective organizational and problem-solving skills.
- Accountable and able to take ownership of your tasks and
projects.
- Experience with Microsoft Office programs and email.
- Ability to work independently after training period.
How to Apply:
For full consideration, please submit the following
document(s):
- A letter of interest describing relevant job experiences as
they relate to the listed job qualifications and interest in the
position
- Curriculum vitae / Resume
- Three to five professional references, including name, address,
phone number (mobile number if appropriate), and email
address
Questions should be directed to:
Megan Kelsey, Megan.Kelsey@childrenscolorado.org
Screening of Applications Begins:
Immediately and closes five (5) days after posting.
Anticipated Pay Range:
The starting salary range (
or hiring range) for this
position has been established as $
24,949.50 to $33,432.50
(calculated for 0.5 FTE).
The above salary range (
or hiring range) represents the
University's good faith and reasonable estimate of the range of
possible compensation at the time of posting. This position may be
eligible for overtime compensation, depending on the level.
Your total compensation goes beyond the number on your paycheck.
The University of Colorado provides generous leave, health plans,
and retirement contributions that add to your bottom line.
Total Compensation
Calculator
Equal Employment Opportunity Statement:
CU is an Equal Opportunity Employer and complies with all
applicable federal, state, and local laws governing
nondiscrimination in employment. We are committed to creating a
workplace where all individuals are treated with respect and
dignity, and we encourage individuals from all backgrounds to
apply, including protected veterans and individuals with
disabilities.
ADA Statement:
The University will provide reasonable accommodations to applicants
with disabilities throughout the employment application process. To
request an accommodation pursuant to the Americans with
Disabilities Act, please contact the Human Resources ADA
Coordinator at
hr.adacoordinator@cuanschutz.edu
.
Background Check Statement:
The University of Colorado Anschutz Medical Campus is dedicated to
ensuring a safe and secure environment for our faculty, staff,
students, and visitors. To assist in achieving that goal, we
conduct background investigations for all prospective
employees.
Vaccination Statement:
CU Anschutz strongly encourages vaccination against the COVID-19
virus and other
vaccine-preventable diseases . If you work, visit, or volunteer
in healthcare facilities or clinics operated by our affiliated
hospital or clinical partners or by CU Anschutz, you will be
required to comply with the vaccination and medical surveillance
policies of the facilities or clinics where you work, visit, or
volunteer, respectively. In addition, if you work in certain
research areas or perform certain safety-sensitive job duties, you
must enroll in the
occupational health medical surveillance program .